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Safety and Pharmacokinetics of UI112 Compared With UIC202611 in Healthy Adults

9 novembre 2026 aggiornato da: Korea United Pharm. Inc.

A Randomized, Open-Label, Single-Dose, 2x2 Crossover Clinical Trial to Compare and Evaluate the Safety and Pharmacokinetics After Subcutaneous Administration of UI112 or UIC202611 in Healthy Adult Subjects

This Phase 1 clinical trial aims to compare the pharmacokinetics and safety of UI112 and UIC202611 (Wegovy), two injectable products containing semaglutide, in healthy adult volunteers.

A total of 44 healthy adults will be randomly assigned to one of two treatment sequences. Each participant will receive a single 0.5 mg subcutaneous injection of UI112 and UIC202611 in separate treatment periods, with a 6-week washout period between administrations.

Blood samples will be collected at scheduled time points to measure semaglutide concentrations and compare how the two products are absorbed and eliminated from the body. Safety will also be assessed through adverse events, physical examinations, vital signs, electrocardiograms, and laboratory tests.

Panoramica dello studio

Stato

Non ancora reclutamento

Descrizione dettagliata

This is a randomized, open-label, single-dose, two-period, two-sequence crossover Phase 1 clinical trial conducted in healthy adult volunteers.

Participants will be randomly assigned to one of two treatment sequences:

  • Sequence A: UIC202611 in Period 1, followed by UI112 in Period 2.
  • Sequence B: UI112 in Period 1, followed by UIC202611 in Period 2.

Each participant will receive a single 0.5 mg dose of semaglutide by subcutaneous injection into the abdomen during each treatment period. A 6-week washout period will separate the two administrations.

Blood samples for pharmacokinetic analysis will be collected before dosing and at scheduled intervals up to 504 hours (Day 22) after each administration. The primary pharmacokinetic endpoints are AUCt and Cmax. Secondary pharmacokinetic endpoints include AUC168h, AUCinf, CL/F, Vz/F, Tmax, and t1/2.

Pharmacokinetic equivalence will be evaluated using the geometric mean ratios of AUCt and Cmax between the test and reference products and their corresponding 90% confidence intervals, with predefined equivalence limits of 80.00% to 125.00%.

Safety assessments will include adverse events, physical examinations, vital signs, 12-lead electrocardiograms, clinical laboratory tests, and blood glucose measurements. A post-study visit will be conducted between Day 43 and Day 47 after the final administration.

Tipo di studio

Interventistico

Iscrizione (Stimato)

44

Fase

  • Fase 1

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Luoghi di studio

    • North Chungcheong
      • Cheongju-si, North Chungcheong, Corea del Sud, 28644
        • Chungbuk National University Hospital
        • Contatto:
          • Chungbuk National University Hospital Clinical Trial Center
          • Numero di telefono: +82-43-269-7284
          • Email: cbnuhctc2@naver.com

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

Da 19 anni a 64 anni (Adulto)

Accetta volontari sani

Sì

Sessi ammissibili allo studio

Tutto

Descrizione

  • Inclusion Criteria:

    1. Healthy adult volunteers aged 19 years or older and younger than 65 years at screening.
    2. Participants with a body weight of 50.0 kg to 100.0 kg (inclusive) and a body mass index (BMI) of 20.0 kg/m² to 29.9 kg/m² (inclusive) at screening.
    3. Participants without congenital diseases or chronic diseases requiring treatment and without pathological symptoms or findings based on a medical examination.
    4. Participants determined to be suitable for participation in the clinical trial based on clinical laboratory tests, vital signs, physical examinations, and 12-lead electrocardiograms (ECGs) performed at screening.
    5. Participants who voluntarily decide to participate after receiving and fully understanding detailed information about the clinical trial, provide written informed consent, and agree to comply with the study requirements throughout the clinical trial.
  • Exclusion Criteria:

    1. Current or past history of clinically significant hepatic, renal, neurological, psychiatric, respiratory, endocrine, hematological, neoplastic, genitourinary, cardiovascular, gastrointestinal, musculoskeletal, or other clinically significant diseases.
    2. Pregnant women (positive urine human chorionic gonadotropin [HCG] test) or breastfeeding women.
    3. History of hypersensitivity reactions, including anaphylaxis or angioedema, or other clinically significant hypersensitivity to the active ingredient, excipients of the investigational products, or other drugs, including GLP-1 receptor agonists.
    4. History of skin diseases (e.g., burns or skin cancer) or skin transplantation that may affect the absorption of the investigational products.
    5. History of acute or chronic pancreatitis.
    6. Personal or family history of medullary thyroid carcinoma (MTC) or multiple endocrine neoplasia type 2 (MEN2).
    7. Clinically significant abnormalities on a 12-lead ECG at screening, including any of the following:
  • QTc interval >450 ms in males or >460 ms in females.

  • PR interval >200 ms.

  • QRS duration >120 ms. 8. Clinically significant abnormalities in clinical laboratory tests at screening, including any of the following:

  • AST, ALT, ALP, gamma-GT, or total bilirubin >2 times the upper limit of normal (ULN).

  • Serum creatinine outside the reference range or estimated glomerular filtration rate (eGFR), calculated using the CKD-EPI equation, <60 mL/min/1.73 m².

  • Lipase or amylase >2 times the ULN.

  • HbA1c ≥6.5%. 9. History of drug abuse or a positive urine drug screening test for drugs of abuse.

    10. Abnormal vital signs measured in a sitting position after at least 3 minutes of rest at screening, including any of the following:

  • Systolic blood pressure ≤90 mmHg or ≥150 mmHg.

  • Diastolic blood pressure ≤60 mmHg or ≥100 mmHg.

  • Pulse rate ≤40 bpm or ≥100 bpm. 11. Use of drugs that induce or inhibit drug-metabolizing enzymes, such as barbiturates, within 1 month before the first administration of the investigational product.

    12. Use of any prescription medication or herbal medicine that may affect the characteristics of the investigational products within 2 weeks before the first administration, or use of any over-the-counter medication or health functional food within 10 days before the first administration. However, participation may be permitted at the investigator's discretion if the medication is not expected to affect the pharmacokinetic characteristics of the investigational products.

    13. Participation in another clinical trial involving administration of an investigational product within 6 months before the first administration in this study. The day following the last administration in the previous clinical trial is considered Day 1.

    14. Donation of whole blood within 2 months, donation of blood components within 1 month, or receipt of a blood transfusion within 1 month before the first administration, or inability to refrain from blood donation from the time of written informed consent until the post-study visit (PSV).

    15. Regular alcohol consumption exceeding 21 units per week within 6 months before the first administration (1 unit = 10 g or 12.5 mL of pure alcohol), or inability to abstain from alcohol from the time of written informed consent until the PSV.

    16. Smoking more than an average of 10 cigarettes per day within 3 months before the first administration, or inability to abstain from smoking from 24 hours before the first administration until the final blood sampling.

    17. Consumption of grapefruit or grapefruit-containing foods within 72 hours before the first administration, or inability to abstain from such foods until the PSV.

    18. Consumption of caffeine-containing foods or beverages (e.g., coffee, green tea, black tea, carbonated beverages, coffee-flavored milk, or energy drinks) within 24 hours before the first administration, or inability to abstain from such products until the final blood sampling.

    19. Engagement in strenuous exercise exceeding the level of normal daily activities within 72 hours before the first administration, or inability to refrain from such exercise until the PSV.

    20. Inability to maintain dietary habits and physical activity levels comparable to normal daily life from the time of written informed consent until the PSV.

    21. Following an abnormal diet that may affect the absorption, distribution, metabolism, or excretion of the investigational products, or consuming foods that may affect drug metabolism.

    22. Change in body weight of 5% or more within the previous 3 months. 23. Participants who, or whose spouse or partner, plan to become pregnant, or who do not use reliable contraception even without pregnancy plans, from the time of written informed consent until 60 days after the final administration of the investigational product. Reliable contraceptive methods include implants or intrauterine devices, sterilization procedures (e.g., vasectomy or tubal ligation), and barrier methods (e.g., condoms, contraceptive diaphragms, vaginal sponges, or cervical caps used in combination).

    24. Presence of tattoos, sunburn, thermal burns, or other skin abnormalities at the administration site, including cuts, bruising, erythema, induration, or tenderness, that may interfere with medical assessments before or after administration of the investigational products.

    25. Participants considered unsuitable for participation in the clinical trial by the investigator for any reason other than the inclusion and exclusion criteria specified above.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Altro
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione incrociata
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Sequence A

Participants will receive a single 0.5 mg subcutaneous dose of UIC202611 (reference product) in Period 1, followed by a single 0.5 mg subcutaneous dose of UI112 (test product) in Period 2, with a 6-week washout period between treatments.

UI112 is the investigational semaglutide product developed by Korea United Pharm. Co., Ltd. A single 0.5 mg dose will be administered subcutaneously in each participant's assigned treatment period.

Altri nomi:
  • UI112

UIC202611 is the reference product, Wegovy (semaglutide), manufactured by Novo Nordisk. A single 0.5 mg dose will be administered subcutaneously in each participant's assigned treatment period.

Altri nomi:
  • Wegovy
Sperimentale: Sequence B

Participants will receive a single 0.5 mg subcutaneous dose of UI112 (test product) in Period 1, followed by a single 0.5 mg subcutaneous dose of UIC202611 (reference product) in Period 2, with a 6-week washout period between treatments.

UI112 is the investigational semaglutide product developed by Korea United Pharm. Co., Ltd. A single 0.5 mg dose will be administered subcutaneously in each participant's assigned treatment period.

Altri nomi:
  • UI112

UIC202611 is the reference product, Wegovy (semaglutide), manufactured by Novo Nordisk. A single 0.5 mg dose will be administered subcutaneously in each participant's assigned treatment period.

Altri nomi:
  • Wegovy

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Area Under the Plasma Concentration-Time Curve From Time Zero to the Last Quantifiable Concentration (AUCt) of Semaglutide
Lasso di tempo: Pre-dose through 504 hours post-dose (Day 1 to Day 22) in each treatment period.

AUCt is the area under the plasma concentration-time curve from time zero to the last quantifiable concentration of semaglutide, calculated using the linear trapezoidal method.

Pre-dose through 504 hours post-dose (Day 1 to Day 22) in each treatment period.
Maximum Observed Plasma Concentration (Cmax) of Semaglutide
Lasso di tempo: Pre-dose through 504 hours post-dose (Day 1 to Day 22) in each treatment period.

Cmax is the maximum observed plasma concentration of semaglutide following a single subcutaneous administration of each study product.

Pre-dose through 504 hours post-dose (Day 1 to Day 22) in each treatment period.

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Area Under the Plasma Concentration-Time Curve From 0 to 168 Hours (AUC168h) of Semaglutide
Lasso di tempo: Pre-dose through 168 hours post-dose (Day 1 to Day 8) in each treatment period.

AUC168h is the area under the plasma concentration-time curve of semaglutide from time zero to 168 hours after dosing.

Pre-dose through 168 hours post-dose (Day 1 to Day 8) in each treatment period.
Area Under the Plasma Concentration-Time Curve From Time Zero to Infinity (AUCinf) of Semaglutide
Lasso di tempo: Pre-dose through 504 hours post-dose (Day 1 to Day 22) in each treatment period.

AUCinf is the area under the plasma concentration-time curve of semaglutide from time zero extrapolated to infinity, calculated by noncompartmental analysis.

Pre-dose through 504 hours post-dose (Day 1 to Day 22) in each treatment period.
Apparent Clearance (CL/F) of Semaglutide
Lasso di tempo: Pre-dose through 504 hours post-dose (Day 1 to Day 22) in each treatment period.

CL/F is the apparent clearance of semaglutide following subcutaneous administration, estimated using noncompartmental pharmacokinetic analysis.

Pre-dose through 504 hours post-dose (Day 1 to Day 22) in each treatment period.
Apparent Volume of Distribution (Vz/F) of Semaglutide
Lasso di tempo: Pre-dose through 504 hours post-dose (Day 1 to Day 22) in each treatment period.

Vz/F is the apparent volume of distribution of semaglutide during the terminal phase following subcutaneous administration, estimated using noncompartmental analysis.

Pre-dose through 504 hours post-dose (Day 1 to Day 22) in each treatment period.
Time to Maximum Observed Plasma Concentration (Tmax) of Semaglutide
Lasso di tempo: Pre-dose through 504 hours post-dose (Day 1 to Day 22) in each treatment period.

Tmax is the observed time required to reach the maximum plasma concentration (Cmax) of semaglutide after dosing.

Pre-dose through 504 hours post-dose (Day 1 to Day 22) in each treatment period.
Terminal Elimination Half-Life (t1/2) of Semaglutide
Lasso di tempo: Pre-dose through 504 hours post-dose (Day 1 to Day 22) in each treatment period.

The terminal elimination half-life of semaglutide is calculated as ln(2)/lambda z, where lambda z is the terminal elimination rate constant estimated from the plasma concentration-time profile.

Pre-dose through 504 hours post-dose (Day 1 to Day 22) in each treatment period.

Altre misure di risultato

Misura del risultato
Misura Descrizione
Lasso di tempo
Number of Participants With Adverse Events (AEs) and Serious Adverse Events (SAEs)
Lasso di tempo: From the first administration through the post-study visit (Day 43 to Day 47 after the final administration).

The number and percentage of participants experiencing adverse events and serious adverse events will be assessed. Adverse events will be summarized by severity, seriousness, and relationship to the study drug.

From the first administration through the post-study visit (Day 43 to Day 47 after the final administration).

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

1 gennaio 2027

Completamento primario (Stimato)

1 novembre 2027

Completamento dello studio (Stimato)

1 dicembre 2027

Date di iscrizione allo studio

Primo inviato

28 ottobre 2026

Primo inviato che soddisfa i criteri di controllo qualità

9 novembre 2026

Primo Inserito (Effettivo)

13 novembre 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

13 novembre 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

9 novembre 2026

Ultimo verificato

1 novembre 2026

Maggiori informazioni

Termini relativi a questo studio

Termini MeSH pertinenti aggiuntivi

Altri numeri di identificazione dello studio

  • KUP-UI112-101

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Descrizione del piano IPD

There is no current plan to share individual participant data (IPD) with external researchers. Study data will be managed by the sponsor in accordance with the study protocol, applicable regulations, and confidentiality requirements.

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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